以上为北京时间。链接检查不代表仍在招聘，申请前请以招聘官网为准。
按这个岗位的城市和方向提醒，确认后才开启，可选择每日或每周。
岗位城市暂未明确，请先到找职位页面选择城市和方向。
选择求职条件制药助理，负责生产线操作、产品质量检查、文档记录、设备清洁及卫生维护。要求高中或同等学历，0-1年制造业经验，标准A/B轮班（晚班6pm-6am），时薪$17.11-$28.51。
ROLE SUMMARY
Performs light inspection and/or a limited number of manual and/or automated manufacturing support functions. Performs verification of defects for development of defect kits. This may include line clearance, outfeed/accumulation, scale operation, overwrap, carton/casing, canning, labeling, capping stoppering, and equipment/machine cleaning and sanitation in compliance with SOPs, cGMPs, batch records, TCPs, BOMs and POPs.
ROLE RESPONSIBILITIES
Operate Dabrico’s, labelers, canning, casers, overwraps, checkweighers, cartoners and other machinery per assigned room.
Ensure product quality during the production process.
Perform line clearances and verify filter MIT’s.
Pull and deliver QC samples.
Check in cages and warehouse materials.
Perform pH testing (in-process) for fill lines and volume testing/leak tests.
Prepare documentation of sterilization and daily tags.
Notify Group Leader/Supervisor of all safety issues.
Maintain proper documentation – batch records, check sheets, logbooks.
Ensure preventative maintenance is current.
Perform all tasks in a safe manner and stay current with training requirements.
Perform room and equipment sanitation.
Equipment/machine cleaning and basic sanitation.
Ensure adherence to all plant safety rules in area of responsibility.
BASIC QUALIFICATIONS
High school diploma or equivalent (GED)
0-1 years experience working in a manufacturing and/or industrial type environment
Able to make minor mechanical machine adjustments.
Must be self-motivated, with a problem-solving mindset.
Ability to work effectively both independently and as a part of a team.
When assigned to a fill line must be aseptically trained.
Must be able to communicate and work well interdepartmentally, as well as, with all plant departments.
Must be able to read and write, as well as follow written and oral instructions.
PHYSICAL/MENTAL REQUIREMENTS
PHYSICAL/MENTAL REQUIREMENTS
Required to do frequent lifting of 15-20 pounds and occasional lifting in excess of 25 pounds.
Vision must be correctable to 20/20.
Must be able to withstand exposure to inks, solvents and liquids.
Stand for up to 8 to 12 hours depending on assigned area.
Must be able to push, pull and/or lift above shoulders.
Push and pull heavy carts or tanks.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Standard A/B schedule.
6pm-6am
Ability to work overtime as needed.
Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Manufacturing
研究和试验发展
负责药品填充室的准备与设备卫生维护，严格遵守批次记录和cGMP规范。确保环境异常控制在可接受范围，保持安全操作并与团队保持良好沟通。需要高中毕业及至少一年制药或制造业经验。
